Gene Expression: RPGR

Gene Data

  • Gene Symbol: RPGR
  • Gene ID: 6103
  • Synonyms: COD1, CORDX1, CRD, PCDX, RP15, RP3, XLRP3, orf15
  • Description: retinitis pigmentosa GTPase regulator
  • Database Refs: HGNC:10295, MIM:312610, Ensembl:ENSG00000156313, HPRD:02425, Vega:OTTHUMG00000021361
  • Links: Allen Brain Atlas,NCBI, GeneCards
Splicing Dynamics: DEXseq identifies changes in 0 out of 22 exons in this gene. (More about DEXSeq here)

Cluster Associations

This gene is associated with the following clusters:

Disease Associations

This gene is associated with the following diseases. Clicking on the disease will take you to the disease association entry for that disease.

This gene is associated with 31 diseases, scroll to view all:
  1. Alstrom syndrome
  2. Bardet-Biedl syndrome
  3. Blindness
  4. cone-rod dystrophy
  5. Congenital stationary night blindness
  6. Disease
  7. Disease of anatomical entity
  8. Eye and adnexa disease
  9. Eye disease
  10. Fundus dystrophy
  11. Genetic disease
  12. Globe disease
  13. Laurence-Moon syndrome
  14. Leber congenital amaurosis
  15. Myopia
  16. Nervous system disease
  17. Night blindness
  18. Ornithine carbamoyltransferase deficienc
  19. Orofaciodigital syndrome
  20. Peripheral retinal degeneration
  21. Primary ciliary dyskinesia
  22. Refractive error
  23. Retinal degeneration
  24. Retinal disease
  25. Retinitis pigmentosa
  26. Senior-Loken syndrome
  27. Sensory system disease
  28. Situs inversus
  29. Suppression amblyopia
  30. Usher syndrome
  31. Visceral heterotaxy

Stage Associations

This gene is associated with the following stages: